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Research 931–960 of 1000+
- A genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair features
- The Harmonies Played by TGF-β in Stem Cell Biology
- An Update of Congenital Adrenal Hyperplasia
- Protoporphyrin IX: the Good, the Bad, and the Ugly
- Hairless triggers reactivation of hair growth by promoting Wnt signaling
- BAC-mediated gene-dosage analysis reveals a role for Zipro1 (Ru49/Zfp38) in progenitor cell proliferation in cerebellum and skin
- Nonalcoholic fatty liver disease and polycystic ovary syndrome
- What causes hidradenitis suppurativa ?—15 years after
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- In vivo function of VDR in gene expression-VDR knock-out mice
- Pathways to inflammation: acne pathophysiology
- Exploiting the Keratin 17 Gene Promoter To Visualize Live Cells in Epithelial Appendages of Mice
- Preparation of hair beads and hair follicle germs for regenerative medicine
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Red Ginseng Extract Promotes the Hair Growth in Cultured Human Hair Follicles
- Chrousos syndrome: from molecular pathogenesis to therapeutic management
- Interactions of the Vitamin D Receptor with the Corepressor Hairless
- No Evidence that 2D:4D is Related to the Number of CAG Repeats in the Androgen Receptor Gene
- Asian Hair: A Review of Structures, Properties, and Distinctive Disorders
- TCL1 transgenic mouse model as a tool for the study of therapeutic targets and microenvironment in human B-cell chronic lymphocytic leukemia
- Morphological Approach to Hair Disorders
- Desmoglein 4 is regulated by transcription factors implicated in hair shaft differentiation
- Histopathological and Ultrastructural Study of Ectodermal Dysplasia/Skin Fragility Syndrome
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- The VEGF +405 G>C 5' untranslated region polymorphism and risk of PCOS: a study in the South Indian Women
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Mutations in the vitamin D receptor gene in four patients with hereditary 1,25-dihydroxyvitamin D-resistant rickets
- Increased Susceptibility to Skin Carcinogenesis Associated with a Spontaneous Mouse Mutation in the Palmitoyl Transferase Zdhhc13 Gene
- AabHLH112, a bHLH transcription factor, positively regulates sesquiterpenes biosynthesis in Artemisia annua
- Characterization of minoxidil/hydroxypropyl-β-cyclodextrin inclusion complex in aqueous alginate gel useful for alopecia management: Efficacy evaluation in male rat